Alfredo Orrico

2.5k total citations
61 papers, 1.7k citations indexed

About

Alfredo Orrico is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Alfredo Orrico has authored 61 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 29 papers in Genetics and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Alfredo Orrico's work include Genetics and Neurodevelopmental Disorders (11 papers), Connective tissue disorders research (7 papers) and Ion channel regulation and function (7 papers). Alfredo Orrico is often cited by papers focused on Genetics and Neurodevelopmental Disorders (11 papers), Connective tissue disorders research (7 papers) and Ion channel regulation and function (7 papers). Alfredo Orrico collaborates with scholars based in Italy, United Kingdom and United States. Alfredo Orrico's co-authors include Lucia Galli, Vincenzo Sorrentino, Antonio Federico, Maria Teresa Dotti, Joussef Hayek, Anita Rauch, Christiane Zweier, André Reis, Emilia K. Bijlsma and Michele Zappella and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and FEBS Letters.

In The Last Decade

Alfredo Orrico

59 papers receiving 1.7k citations

Peers

Countries citing papers authored by Alfredo Orrico

Since Specialization

Citations

This map shows the geographic impact of Alfredo Orrico's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Alfredo Orrico with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alfredo Orrico more than expected).

Fields of papers citing papers by Alfredo Orrico

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alfredo Orrico. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Alfredo Orrico. The network helps show where Alfredo Orrico may publish in the future.

Co-authorship network of co-authors of Alfredo Orrico

This figure shows the co-authorship network connecting the top 25 collaborators of Alfredo Orrico. A scholar is included among the top collaborators of Alfredo Orrico based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Alfredo Orrico. Alfredo Orrico is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Case report: The CCDC103 variant causes ultrastructural sperm axonemal defects and total sperm immotility in a professional athlete without primary ciliary diskinesia 2023 ·Frontiers in Genetics ·(unknown), Alice Luddi, (unknown), (unknown), (unknown), Eugenio Paccagnini, Mariangela Gentile, Pietro Lupetti, (unknown), Alfredo Orrico, Liborio Stuppia, Paola Piomboni	2
2	The Variable Expression of a Novel MBD5 Gene Frameshift Mutation in an Italian Family 2020 ·Neuropediatrics ·Alfredo Orrico, Lucia Galli, (unknown), (unknown), (unknown), (unknown)	1
3	Clinical utility gene card for: Aarskog–Scott Syndrome (faciogenital dysplasia) – update 2015 2014 ·European Journal of Human Genetics ·Alfredo Orrico, Lucia Galli, Jill Clayton‐Smith, Jean‐Pierre Fryns	12
4	An additional case of cerebrofaciothoracic dysplasia associated with Chiari type I malformation 2013 ·Clinical Dysmorphology ·(unknown), (unknown), (unknown), Giuseppina Marseglia, Chiara Pescucci, (unknown), Francesca Torricelli, Alfredo Orrico	7
5	CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila 2009 ·The American Journal of Human Genetics ·Christiane Zweier, Eiko K. de Jong, Markus Zweier, Alfredo Orrico, Lilian Bomme Ousager, Amanda Collins, Emilia K. Bijlsma, Merel A.W. Oortveld, Arif B. Ekici, André Reis, Annette Schenck, Anita Rauch	244
6	Novel PTEN mutations in neurodevelopmental disorders and macrocephaly 2009 ·Clinical Genetics ·Alfredo Orrico, (unknown), Sabrina Buoni, A Orsi, (unknown), Vincenzo Sorrentino	81
7	Haploinsufficiency of TCF4 Causes Syndromal Mental Retardation with Intermittent Hyperventilation (Pitt-Hopkins Syndrome) 2007 ·The American Journal of Human Genetics ·Christiane Zweier, Maarit Peippo, Juliane Hoyer, Sérgio B. Sousa, Armand Bottani, Jill Clayton‐Smith, William Reardon, Jorge Saraiva, (unknown), (unknown), Koenraad Devriendt, Thomy de Ravel, Emilia K. Bijlsma, Raoul C. M. Hennekam, Alfredo Orrico, Monika Cohen, Alexander Dreweke, André Reis, (unknown), Anita Rauch	215
8	Unusually severe expression of craniofacial features in Aarskog‐Scott syndrome due to a novel truncating mutation of the FGD1 gene 2006 ·American Journal of Medical Genetics Part A ·Alfredo Orrico, Lucia Galli, María Gabriela Obregón, (unknown), (unknown), Vincenzo Sorrentino	21
9	Cortical damage in brains of patients with adult-form of myotonic dystrophy type 1 and no or minimal MRI abnormalities 2006 ·Journal of Neurology ·Antonio Giorgio, Maria Teresa Dotti, Marco Battaglini, Silvia Marino, Marzia Mortilla, Maria Laura Stromillo, Placido Bramanti, Alfredo Orrico, Antonio Federico, Nicola De Stefano	25
10	Attention‐deficit/hyperactivity disorder (ADHD) and variable clinical expression of Aarskog–Scott syndrome due to a novel FGD1 gene mutation (R408Q) 2005 ·American Journal of Medical Genetics Part A ·Alfredo Orrico, Lucia Galli, Sabrina Buoni, Joussef Hayek, Anna Luchetti, Stefania Lorenzini, Michele Zappella, Maria Grazia Pomponi, Vincenzo Sorrentino	25
11	Autonomic Dysfunction in Mental Retardation and Spastic Paraparesis With MECP2 Mutation 2004 ·Journal of Child Neurology ·Maria Teresa Dotti, Francesca Guideri, Maurizio Acampa, Alfredo Orrico, Carla Battisti, Antonio Federico	8
12	Retinochoroidal atrophy in two adult patients with Angelman syndrome 2003 ·American Journal of Medical Genetics Part A ·Alessandra Rufa, Maria Teresa Dotti, Alfredo Orrico, Carla Battisti, (unknown), Antonio Federico	10
13	Septo‐optic dysplasia with digital anomalies associated with maternal multidrug abuse during pregnancy 2002 ·European Journal of Neurology ·Alfredo Orrico, Lucia Galli, Michele Zappella, Lucia Monti, (unknown), Carlo Venturi, Joussef Hayek	21
14	MECP2 mutation in male patients with non‐specific X‐linked mental retardation 2000 ·FEBS Letters ·Alfredo Orrico, Ching‐Wan Lam, Lucia Galli, Maria Teresa Dotti, Joussef Hayek, Sui-Fan Tong, Priscilla M.K. Poon, Michele Zappella, Antonio Federico, Vincenzo Sorrentino	183
15	Mutations in the glucose‐6‐phosphate transporter (G6PT) gene in patients with glycogen storage diseases type 1b and 1c 1999 ·FEBS Letters ·Lucia Galli, Alfredo Orrico, Paola Marcolongo, Rosella Fulceri, Ann N. Burchell, Daniela Melis, Rossella Parini, Rosanna Gatti, Ching‐Wan Lam, Angelo Benedetti, Vincenzo Sorrentino	43
16	Mosaicism for full mutation and normal-sized allele of the FMR1 gene: A new case 1998 ·American Journal of Medical Genetics ·Alfredo Orrico, Lucia Galli, (unknown), Katrin Plewnia, Stefano Censini, Antonio Federico	29
17	An additional case of craniodigital syndrome: variable expression of the Filippi syndrome? 1997 ·Clinical Genetics ·Alfredo Orrico, Joussef Hayek	6
18	Benzodiazepines Inhibit in Vitro Free Radical Formation from Human Neutrophils Induced by Fmlp and A23187. 1987 ·Immunopharmacology and Immunotoxicology ·(unknown), L. Ceccatelli, Pier Leopoldo Capecchi, Alfredo Orrico, A. L. Pasqui, T. Di Perri	12
19	Receptors on the neutrophil membrane. I. Flunarizine-adenosine antagonism as detected by 1H-nuclear magnetic resonance relaxation investigations 1987 ·Biophysical Journal ·T. Di Perri, Alfredo Orrico, (unknown), Elena Gaggelli, Gianni Valensin	5
20	Polymorphonuclear leucocytes as a model of Ca++ and Mg++-dependent cellular activation. Effect of calcium entry blockers. 1985 ·PubMed ·T. Di Perri, Franco Laghi‐Pasini, Anna Laura Pasqui, L. Ceccatelli, Alfredo Orrico, P.L. Capecchi	6

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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